Prospective CoHoRt Of Non-infectious Intermediate, pOsterior or panuveitiS

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorCentre Hospitalier National d'Ophtalmologie des Quinze-Vingts

About this trial

prospective, cohort, longitudinal, multicenter, non-randomized study of patients with non-infectious posterior segment uveitis or panuveitis, with a group of control patients (scheduled for cataract or vitreoretinal surgery) and constitution of biological collection.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Adult patients (≥ 18 years);

Non-infectious uveitis;

Intermediate, posterior or panuveitis;

Systemic corticosteroids or periocular or intravitreal injections of corticosteroids;

Disqualifiers

Isolated anterior uveitis ;

Absence of inflammatory chorioretinal and/or inflammatory retinal vascular lesion;

Anterior chamber cell grade< 0.5+;

Vitreous haze grade <0.5+;

Trial design

Design model

Parallel

Treatments tested in this trial

  • care strategy

    Diagnostic test

    Uveitis patients: * Blood sample (20ml): Additional 20 ml blood sample during the first visit and potentially during follow-up (if necessary) for the purpose of the biological collection; * Ocular sample (aqueous humor, vitreous): if required by the clinical context for the needs of the biological collection; * Specific imaging: adaptive optics or Doppler holography, these procedures will be indicated on a case-by-case basis, at the investigator's discretion, and concern only patients with inflammatory vascular damage (5 to 10% of patients in the uveitis cohort); * Quality of Life NEI-VFQ 25: provided at the inclusion visit and at follow-up visits M3-V2, M12-V5 and M24-V7.

Treatment groups

2,000 Participants
are divided into 2 treatment groups
Group A: Uveitis PatientsExperimental treatment 1 intervention
Group B: Control PatientsActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Imaging database development

To develop an imaging database of Non-Infectious Uveitis of the posterior segment (NIUPS) using multimodal imaging

Time frame
60 months
2

Biological constitution

To Constitute a biological collection of ocular and blood samples of NIUPS patients and controls

Time frame
60 months
3

medico economic costs estimation

To estimate the current costs of treatment by ensuring linkage of cohort patients to the national claims database

Time frame
60 months

Secondary outcomes

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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